地红霉素结构式
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常用名 | 地红霉素 | 英文名 | Dirithromycin |
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CAS号 | 62013-04-1 | 分子量 | 835.074 | |
密度 | 1.2±0.1 g/cm3 | 沸点 | 871.8±65.0 °C at 760 mmHg | |
分子式 | C42H78N2O14 | 熔点 | 185 - 189ºC | |
MSDS | 中文版 美版 | 闪点 | 481.0±34.3 °C | |
符号 |
GHS07 |
信号词 | Warning |
地红霉素用途Dirithromycin(LY 237216)是大环内酯类糖肽抗生素,能与细菌核糖体70S中的50S亚基相结合。 |
中文名 | 地红霉素 |
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英文名 | dirithromycin |
中文别名 | [9S(R)]-9-脱氧-11-脱氧-9,11-[亚氨[2-(2-甲氧基乙氧基)亚乙基]氧]红霉素 | 布大卡因 | [9S]-9-去氧-11-脱氧-9,11-[亚氨[2-(2-甲氧基乙氧基)亚乙基]氧]红霉素 | [9S(R)]-9-脱氧-11-脱氧-9,11-[亚胺基[2-(2-甲氧基乙氧基)乙叉基]氧基]红霉素 |
英文别名 | 更多 |
描述 | Dirithromycin(LY 237216)是大环内酯类糖肽抗生素,能与细菌核糖体70S中的50S亚基相结合。 |
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相关类别 | |
参考文献 |
密度 | 1.2±0.1 g/cm3 |
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沸点 | 871.8±65.0 °C at 760 mmHg |
熔点 | 185 - 189ºC |
分子式 | C42H78N2O14 |
分子量 | 835.074 |
闪点 | 481.0±34.3 °C |
精确质量 | 834.545288 |
PSA | 196.33000 |
LogP | 2.84 |
外观性状 | 晶体 |
蒸汽压 | 0.0±0.6 mmHg at 25°C |
折射率 | 1.533 |
储存条件 | -20°C |
分子结构 | 1、 摩尔折射率:217.28 2、 摩尔体积(cm3/mol):691.6 3、 等张比容(90.2K):1854.8 4、 表面张力(dyne/cm):51.7 5、 极化率(10-24cm3):86.13 |
更多 | 从乙醇-水结晶,熔点186~189℃(分解)。pKa9.0(66%二甲基氟化物水溶液)。急性毒性LD50小鼠(g/kg):>1皮下注射,>1口服。 |
下列化合物和2-(2-甲氧基乙氧基)乙醛,在乙醇中于室温下搅拌24h;或者和2-(2-甲氧基乙氧基)乙醛的甲缩醛或乙缩醛,在二氧六环-水中,Dowex 50W存在下,在室温下搅拌6h,均可得到地红霉素。
海关编码 | 29419000 |
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The new macrolide antibiotics: azithromycin, clarithromycin, dirithromycin, and roxithromycin.
Ann. Pharmacother. 26(1) , 46-55, (1992) To review the chemistry, antimicrobial spectrum, pharmacokinetics, clinical trials, adverse effects, and drug interactions of four new macrolide antibiotics: azithromycin, clarithromycin, dirithromyci... |
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Pharmacokinetics of dirithromycin.
J. Antimicrob. Chemother. 31 Suppl C , 65-75, (1993) Dirithromycin is a new member of the macrolide class of antibiotics and has been developed for oral administration. Dirithromycin is a 14-membered lactone ring macrolide and is the C9-oxazine derivati... |
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Modulation of human polymorphonuclear neutrophil function by macrolides: preliminary data concerning dirithromycin.
J. Antimicrob. Chemother. 31 Suppl C , 51-64, (1993) Polymorphonuclear neutrophils (PMN) play a prominent role in the host response to infectious diseases. One major bactericidal mechanism used by these cells is the production of reactive oxygen species... |
(2R,3R,6R,7S,8S,9R,10R,12R,13S,15R,17S)-3-Ethyl-2,10-dihydroxy-15-[(2-methoxyethoxy)methyl]-2,6,8,10,12,17-hexamethyl-5-oxo-9-{[3,4,6-trideoxy-3-(dimethylamino)-β-D-xylo-hexopyranosyl]oxy}-4,16-dio xa-14-azabicyclo[11.3.1]heptadec-7-yl 2,6-dideoxy-3-C-methyl-3-O-methyl-α-L-ribo-hexopyranoside |
Noriclan |
Dynabac |
Dirythromycin |
4,16-Dioxa-14-azabicyclo[11.3.1]heptadecan-5-one |
MFCD00865041 |
ASE 136 |
4,16-Dioxa-14-azabicyclo[11.3.1]heptadecan-5-one, 7-[(2,6-dideoxy-3-C-methyl-3-O-methyl-α-L-ribo-hexopyranosyl)oxy]-3-ethyl-2,10-dihydroxy-15-[(2-methoxyethoxy)methyl]-2,6,8,10,12,17-hexamethyl-9- [[3,4,6-trideoxy-3-(dimethylamino)-β-D-xylo-hexopyranosyl]oxy]-, (2R,3R,6R,7S,8S,9R,10R,12R,13S,15R,17S)- |
Dirithomycin |
Valodin |
Dirithromycin |
Antibiotic AS-E 136 |